Plasma Amyloid-β dynamics in late-life major depression: a longitudinal study

被引:21
作者
Pomara, Nunzio [1 ,2 ]
Bruno, Davide [3 ]
Plaska, Chelsea Reichert [1 ,4 ]
Ramos-Cejudo, Jaime [4 ]
Osorio, Ricardo S. [1 ,4 ]
Pillai, Anilkumar [5 ,6 ,7 ]
Imbimbo, Bruno P. [8 ]
Zetterberg, Henrik [9 ,10 ,11 ,12 ,13 ]
Blennow, Kaj [11 ,12 ]
机构
[1] Nathan S Kline Inst Psychiat Res, Orangeburg, NY 10962 USA
[2] NYU, Dept Psychiat & Pathol, Grossman Sch Med, New York, NY 10016 USA
[3] Liverpool John Moores Univ, Sch Psychol, Liverpool, Merseyside, England
[4] NYU, Dept Psychiat, Grossman Sch Med, 550 1St Ave, New York, NY 10016 USA
[5] Univ Texas Hlth Sci Ctr Houston UTHlth, McGovern Med Sch, Faillace Dept Psychiat & Behav Sci, Pathophysiol Neuropsychiat Disorders Program, Houston, TX USA
[6] Charlie Norwood VA Med Ctr, Res & Dev, Augusta, GA USA
[7] Augusta Univ, Med Coll Georgia, Dept Psychiat & Hlth Behav, Augusta, GA USA
[8] Chiesi Farmaceut, Res & Dev, Parma, Italy
[9] UCL Inst Neurol, Dept Neurodegenerat Dis, London, England
[10] UK Dementia Res Inst UCL, London, England
[11] Univ Gothenburg, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Sahlgrenska Acad, Molndal, Sweden
[12] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[13] Hong Kong Ctr Neurodegenerat Dis, Clear Water Bay, Hong Kong, Peoples R China
基金
瑞典研究理事会; 欧洲研究理事会;
关键词
ALZHEIMER-DISEASE; COGNITIVE DECLINE; RISK-FACTOR; EARLY-ONSET; SYMPTOMS; DEPOSITION; HISTORY; DEMENTIA; PLAQUES; TANGLES;
D O I
10.1038/s41398-022-02077-8
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Depressed individuals are twice as likely to develop Alzheimer's disease (AD) as compared to controls. Brain amyloid-beta (A beta) deposition is believed to have a major role in AD pathogenesis but studies also suggest associations of A beta dynamics and depression. The aim of this study was to test if plasma A beta levels are longitudinally associated to late-life depression. We measured plasma levels of amyloid-beta(1-40) (A beta 40) and amyloid-beta(1-42) (A beta 42) peptides longitudinally for three consecutive years in 48 cognitively intact elderly subjects with late-life major depressive disorder (LLMD) and 45 age-matched cognitively healthy controls. We found that the A beta 42/A beta 40 plasma ratio was significantly and steadily lower in depressed subjects compared to controls (p < 0.001). At screening, A beta 42/A beta 40 plasma did not correlate with depression severity (as measured with Hamilton Depression Scale) or cognitive performance (as measured with Mini-Mental State Examination) but was associated to depression severity at 3 years after adjustment for age, education, cognitive performance, and antidepressants use. This study showed that reduced plasma A beta 42/A beta 40 ratio is consistently associated with LLMD diagnosis and that increased severity of depression at baseline predicted low A beta 42/A beta 40 ratio at 3 years. Future studies are needed to confirm these findings and examine if the consistently lower plasma A beta 42/A beta 40 ratio in LLMD reflects increased brain amyloid deposition, as observed in AD subjects, and an increased risk for progressive cognitive decline and AD.
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页数:7
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共 53 条
[1]   Brain-Derived Neurotrophic Factor and Neuropsychiatric Disorders [J].
Autry, Anita E. ;
Monteggia, Lisa M. .
PHARMACOLOGICAL REVIEWS, 2012, 64 (02) :238-258
[2]   Increased neural activity during overt and continuous semantic verbal fluency in major depression: mainly a failure to deactivate [J].
Backes, Heidelore ;
Dietsche, Bruno ;
Nagels, Arne ;
Stratmann, Mirjam ;
Konrad, Carsten ;
Kircher, Tilo ;
Krug, Axel .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2014, 264 (07) :631-645
[3]   Depressed Mood is Not a Risk Factor for Incident Dementia in a Community-Based Cohort [J].
Becker, James T. ;
Chang, Yue-Fang ;
Lopez, Oscar L. ;
Dew, Mary Amanda ;
Sweet, Robert A. ;
Barnes, Deborah ;
Yaffe, Kristine ;
Young, Jeffrey ;
Kuller, Lewis ;
Reynolds, Charles F. .
AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2009, 17 (08) :653-663
[4]   Biomarkers for Alzheimer's disease: current status and prospects for the future [J].
Blennow, K. ;
Zetterberg, H. .
JOURNAL OF INTERNAL MEDICINE, 2018, 284 (06) :643-663
[5]   Depression and risk of developing dementia [J].
Byers, Amy L. ;
Yaffe, Kristine .
NATURE REVIEWS NEUROLOGY, 2011, 7 (06) :323-331
[6]   proBDNF Accelerates Brain Amyloid-β Deposition and Learning and Memory Impairment in APPswePS1dE9 Transgenic Mice [J].
Chen, Jia ;
Zhang, Tao ;
Jiao, Shusheng ;
Zhou, Xinfu ;
Zhong, Jinhua ;
Wang, Yanjiang ;
Liu, Juan ;
Deng, Juan ;
Wang, Shuiping ;
Xu, Zhiqiang .
JOURNAL OF ALZHEIMERS DISEASE, 2017, 59 (03) :941-949
[7]   PLATELETS ARE THE PRIMARY SOURCE OF AMYLOID BETA-PEPTIDE IN HUMAN BLOOD [J].
CHEN, M ;
INESTROSA, NC ;
ROSS, GS ;
FERNANDEZ, HL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 213 (01) :96-103
[8]   Depressive symptoms, sex, and risk for Alzheimer's disease [J].
Dal Forno, G ;
Palermo, MT ;
Donohue, JE ;
Karagiozis, H ;
Zonderman, AB ;
Kawas, CH .
ANNALS OF NEUROLOGY, 2005, 57 (03) :381-387
[9]   Corticosterone and related receptor expression are associated with increased β-amyloid plaques in isolated Tg2576 mice [J].
Dong, H. ;
Yuede, C. M. ;
Yoo, H. -S. ;
Martin, M. V. ;
Deal, C. ;
Mace, A. G. ;
Csernansky, J. G. .
NEUROSCIENCE, 2008, 155 (01) :154-163
[10]   Corticotrophin Releasing Factor Accelerates Neuropathology and Cognitive Decline in a Mouse Model of Alzheimer's Disease [J].
Dong, Hongxin ;
Murphy, Keely M. ;
Meng, Liping ;
Montalvo-Ortiz, Janitza ;
Zeng, Ziling ;
Kolber, Benedict J. ;
Zhang, Shanshan ;
Muglia, Louis J. ;
Csernansky, John G. .
JOURNAL OF ALZHEIMERS DISEASE, 2012, 28 (03) :579-592